# congenital stationary night blindness 1D

> congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the SLC24A1 gene on chromosome 15q22

**Wikidata**: [Q32144064](https://www.wikidata.org/wiki/Q32144064)  
**Source**: https://4ort.xyz/entity/congenital-stationary-night-blindness-1d


## References

1. Disease Ontology
2. UniProt
3. A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29